Семейный случай редкой наследственной моторно-сенсорной нейропатии типа 2P, обусловленной мутацией гена LRSAM1
Аннотация
Об авторах
О. А. ЩагинаРоссия
Е. Л. Дадали
Россия
В. П. Федотов
Россия
О. П. Рыжкова
Россия
А. Л. Чухрова
Россия
Т. Б. Миловидова
Россия
А. В. Поляков
Россия
Список литературы
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Для цитирования:
Щагина О.А., Дадали Е.Л., Федотов В.П., Рыжкова О.П., Чухрова А.Л., Миловидова Т.Б., Поляков А.В. Семейный случай редкой наследственной моторно-сенсорной нейропатии типа 2P, обусловленной мутацией гена LRSAM1. Медицинская генетика. 2018;17(8):38-42. https://doi.org/10.25557/2073-7998.2018.08.38-42
For citation:
Shchagina O.A., Dadali E.L., Fedotov V.P., Ryzhkova O.P., Chucrova A.L., Milovidova T.B., Polyakov A.V. Family case of rare Charcot-Marie-Tooth 2P disease caused by LRSAM1 mutation. Medical Genetics. 2018;17(8):38-42. (In Russ.) https://doi.org/10.25557/2073-7998.2018.08.38-42